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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

Carsten G. Bönnemann

Division of Neurology and Neuromuscular Program

The Children's Hospital of Philadelphia




Name/email consistency: high



  • Division of Neurology and Neuromuscular Program, The Children's Hospital of Philadelphia, Philadelphia, USA. 2005
  • Division of Neurology, Children's Hospital of Philadelphia and University of Pennsylvania School of Medicine, 34th Strteet and Civic Center Boulevard, Philadelphia, USA. 2003 - 2004
  • Division of Genetics, Children's Hospital, Howard Hughes Medical Institute, USA. 2002


  1. Limb-girdle muscular dystrophy in childhood. Bönnemann, C.G. Pediatr. Ann (2005) [Pubmed]
  2. Myopathies resulting from mutations in sarcomeric proteins. Bönnemann, C.G., Laing, N.G. Curr. Opin. Neurol. (2004) [Pubmed]
  3. Filamin C accumulation is a strong but nonspecific immunohistochemical marker of core formation in muscle. Bönnemann, C.G., Thompson, T.G., van der Ven, P.F., Goebel, H.H., Warlo, I., Vollmers, B., Reimann, J., Herms, J., Gautel, M., Takada, F., Beggs, A.H., Fürst, D.O., Kunkel, L.M., Hanefeld, F., Schröder, R. J. Neurol. Sci. (2003) [Pubmed]
  4. Primary gamma-sarcoglycanopathy (LGMD 2C): broadening of the mutational spectrum guided by the immunohistochemical profile. Bönnemann, C.G., Wong, J., Jones, K.J., Lidov, H.G., Feener, C.A., Shapiro, F., Darras, B.T., Kunkel, L.M., North, K.N. Neuromuscul. Disord. (2002) [Pubmed]
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